CURRENT ETHICAL & REGULATORY REQUIREMENTS FOR
AN AWARENESS PROGRAM
WHENMay 10, 2016, 9am-6pm
ANIIMS, Port Blair
To strengthen and empower the IEC members, clinicians and investigators to ensure that they understand scientific, regulatory norms, ethical design, conduct and reporting of clinical research that will be of uniform nature and meets national and international quality standards.
CLINICAL DEVELOPMENT SERVICES AGENCY (CDSA)
( An extramural unit of THSTI), Dept. of Biotechnology, Ministry of Science & Technology,Government of India
LOCAL ORGANISING SECRETARY
DR. C. DINESH M. NAIDU
Professor & Head of Pharmacology,
ANIIMS, Port Blair.
No Registration Fee
WHO CAN ATTEND
Members from Ethics Committees, Clinicians, Investigators, Clinical research team members.
Create an awareness about current guidelines & regulations for the conduct of clinical research in India so as to
ensure that the trial subject's right, safety and well-being are well protected.
• Ethics Committee Members
• Clinical Investigators